Comfort Home Care
APRIL 18, 2024
In this article, we share vital information about Parkinson’s Disease, the role in-home care can have in managing its challenges, and the qualities to seek in an in-home care provider. Living with Parkinson’s Disease presents numerous challenges, but you don’t have to face them alone.
AlayaCare
MAY 8, 2023
How easily does your system make it for you to see if caregivers are completing activities of daily living (ADLs) on-site? Can you easily export data out of your current system to inform business decisions (i.e., All completed tasks are date and time-stamped within the system for full stakeholder visibility.
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Hospice Nurse Hero
AUGUST 21, 2022
Please read full disclosure for more information. You’re like the detective gathering all the clues ( information ) from the past several months to support changes in the patient’s condition. You can also use the information from your admission and previous interdisciplinary group (IDG) meetings to help you document.
AlayaCare
APRIL 11, 2019
No paper or timesheets : Well-designed software means caregivers never have to manually record any client information or drive to the office to clock in or out. Real-time information and communication: No more dealing with lost forms, incomplete information, or unknown situations.
Hospice Nurse Hero
MARCH 6, 2024
Requires assistance with ADLs. Disease-Specific Declines: Each condition presents unique markers of decline. This can include worsening symptoms, decreased functional status, or increased dependence on ADLs. Subjective Data: This information comes from your patients, families, caregivers, and friends. Denies pain.
Hospice Nurse Hero
JANUARY 26, 2022
Please read full disclosur e for more information. As a hospice nurse, you should: Document at the bedside : First to ensure accuracy then to make sure the team has the information they need to care for the patient. ( Chart all calls: Phone calls and triage notes inform the team. This post may contain affiliate links.
GeriPal
OCTOBER 26, 2023
And a lot of them never actually improve their ADLs once they’re sent to SNF. Lynn: If they need to go somewhere and receive ADL support and supportive care at the same time, there’s no mechanism to pay for that. We need that information. This information is so vital. Sarguni: Yeah. Eric: Yeah.
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